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福替考洛斯研究 - 使用牛初乳作为强化剂增强极早产儿母乳营养的多中心研究:一项随机对照预试验研究方案。

FortiColos - a multicentre study using bovine colostrum as a fortifier to human milk in very preterm infants: study protocol for a randomised controlled pilot trial.

机构信息

Section of Comparative Pediatrics and Nutrition, IVH, University of Copenhagen, Frederiksberg, Denmark.

University of Southern Denmark, Odense, Denmark.

出版信息

Trials. 2019 May 22;20(1):279. doi: 10.1186/s13063-019-3367-7.

Abstract

BACKGROUND

Very preterm infants (< 32 weeks gestation) have a relatively high nutrient requirement for growth and development. The composition of human milk is often inadequate to ensure optimal growth so it is common to fortify human milk for very preterm infants with nutrient fortifiers based on bovine milk. However, there are concerns that bovine milk-based fortifiers may increase the risk of feeding intolerance, necrotizing enterocolitis and late-onset sepsis. We hypothesize that a bovine colostrum-based product is a suitable alternative to bovine milk-based products when used as a fortifier to human milk in very preterm infants.

METHODS/DESIGN: In an open-label multicentre randomised controlled pilot trial, 200 very preterm infants (26 + 0 to 30 + 6 weeks gestation at birth) will be randomly allocated to a bovine colostrum-based or a bovine milk-based fortifier added to mother's own milk and/or human donor milk. Outcomes are growth rate, incidence of necrotizing enterocolitis and late-onset sepsis, a series of paraclinical endpoints, and practical feasibility of using the novel fortifier for very preterm infants.

DISCUSSION

The optimal enteral diet and feeding regimen for very preterm infants remain debated; this clinical trial will document the feasibility, safety and preliminary efficacy of using bovine colostrum, rich in nutrients and bioactive factors, as a novel fortifier for human milk to very preterm infants. Data on infant growth, metabolism, gut function and immunity will be assessed from clinical data as well as blood and stool samples.

TRIAL REGISTRATION

Registered retrospectively 25 May 2018 at ClinicalTrials.gov: NCT03537365 .

摘要

背景

极早产儿(<32 周胎龄)的生长和发育需要相对较高的营养需求。人乳的成分往往不足以确保最佳生长,因此通常使用基于牛乳的营养强化剂来强化极早产儿的人乳。然而,人们担心基于牛乳的强化剂可能会增加喂养不耐受、坏死性小肠结肠炎和晚发性败血症的风险。我们假设,当用作极早产儿人乳的强化剂时,牛初乳基产品是基于牛乳产品的合适替代品。

方法/设计:在一项开放标签、多中心随机对照试验中,将 200 名极早产儿(出生时 26+0 至 30+6 周妊娠)随机分配到添加牛初乳基或基于牛乳的强化剂的母亲自身的母乳和/或人捐赠母乳中。结局为生长速度、坏死性小肠结肠炎和晚发性败血症的发生率、一系列临床前终点以及新型强化剂在极早产儿中的实际可行性。

讨论

极早产儿的最佳肠内饮食和喂养方案仍存在争议;本临床试验将记录使用富含营养和生物活性因子的牛初乳作为人乳的新型强化剂用于极早产儿的可行性、安全性和初步疗效。将从临床数据以及血液和粪便样本中评估婴儿的生长、代谢、肠道功能和免疫情况。

试验注册

于 2018 年 5 月 25 日在 ClinicalTrials.gov 上进行回顾性注册:NCT03537365。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/6530095/57988833edf5/13063_2019_3367_Fig1_HTML.jpg

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